510(k) K001721
K001721 is an FDA 510(k) premarket notification submitted by Pasco Laboratories, Inc. for the device "PASCO MIC AND MIC/ID PANELS". The FDA issued a decision of Substantially Equivalent on Aug 4, 2000. The device falls under product code LTT (Panels, Test, Susceptibility, Antimicrobial), a Class II device regulated under 21 CFR 866.1640. Pasco Laboratories, Inc. has 65 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Aug 4, 2000
- Date Received
- Jun 6, 2000
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- Panels, Test, Susceptibility, Antimicrobial
- Device Class
- Class II
- Regulation Number
- 866.1640
- Review Panel
- MI
- Submission Type
- 510(k)